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Guido D. Pollevick

Clinical Data, Inc

27

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Increased Carrier Detection With Expanded Carrier Screening in Multiple Ancestries [7O]

2019 Obstetrics & Gynecology
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Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variant

2012 Heart Rhythm
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Abstract 16035: Epidemiological Evidence Suggests CAV3 T78M Should be Considered a Benign Polymorphism and not an Independent, Multi-Disease-Susceptibility Mutation

2011 Circulation
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Abstract 16937: Age at Genetic Testing is Negatively Correlated with the Number of Mutations Found in Five Cardiac Channelopathies and Cardiomyopathies

2011 Circulation
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An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

2010 Heart Rhythm
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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death

2010 Heart Rhythm
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KCNH2-K897T Polymorphism Increases the Risk of Life-Threatening Arrhythmias Following Acute Myocardial Infarction

2010 Heart Rhythm
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Dual Variations in SCN5A and CACNB2b Underlie Cardiac Conduction Disease without Brugada Syndrome

2009 Biophysical Journal
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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation.

2008 Heart Rhythm
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Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

2007 Heart Rhythm
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Citations (63)